Canonical Allele Identifier: CA10859242
Gene: PARP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226363477A>G , CM000663.2:g.226363477A>G GRCh38
NC_000001.10:g.226551178A>G , CM000663.1:g.226551178A>G GRCh37
NC_000001.9:g.224617801A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366794.10:c.2787-317T>C MANE Select ENSP00000355759.5:n.2787-317T>C
ENST00000498787.2:n.4342T>C
ENST00000676481.1:n.232-317T>C
ENST00000676565.1:n.2559-317T>C
ENST00000676685.1:n.4904T>C
ENST00000676709.1:n.3477T>C
ENST00000677091.1:c.*1469-317T>C ENSP00000504745.1:n.*1469-317T>C
ENST00000677189.1:n.840-317T>C
ENST00000677203.1:c.2658-317T>C ENSP00000503396.1:n.2658-317T>C
ENST00000677374.1:n.4438T>C
ENST00000677815.1:n.2679T>C
ENST00000677884.1:n.3599-317T>C
ENST00000677985.1:n.777-317T>C
ENST00000678144.1:c.*1607-317T>C ENSP00000504430.1:n.*1607-317T>C
ENST00000678226.1:n.1766-317T>C
ENST00000678288.1:n.912-317T>C
ENST00000678560.1:c.*2775-317T>C ENSP00000503293.1:n.*2775-317T>C
ENST00000678781.1:n.4439-317T>C
ENST00000679276.1:n.3943-317T>C
ENST00000366794.9:c.2787-317T>C ENSP00000355759.5:n.2787-317T>C
ENST00000463968.5:n.431-317T>C
ENST00000490921.5:n.2742-317T>C
NM_001618.3:c.2787-317T>C NP_001609.2:n.2787-317T>C
NM_001618.4:c.2787-317T>C MANE Select NP_001609.2:n.2787-317T>C
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